CEL-SCI Corporation (NYSE MKT: CVM) reports financial results for the fiscal quarter ended December 31, 2012. CEL-SCI reported that net loss available to shareholders for the quarter ended December 31, 2012 was ($2,310,246) versus ($4,156,833) during the same quarter ended December 31, 2011. Net loss per common share, (basic) was ($0.01) for the quarter ended December 31, 2012 versus ($0.02) during the same quarter ended December 31, 2011. The operating loss for the quarter ended December 31, 2012 was ($5,044,457) versus an operating loss of ($4,443,276) during the same quarter ended December 31, 2011. R&D expenses for the quarter ended December 31, 2012 totaled $2,924,722 versus R&D expenses of $2,456,185 for the quarter ended December 31, 2011. R&D expenses increased because of the increased level of activity associated with conducting the Company’s Phase III clinical study. The Company ended the December quarter with approximately $10,736,000 in cash and cash equivalents. During the quarter, the Company completed a Registered Direct financing, generating net proceeds of $9,807,000. Geert Kersten, Chief Executive Officer said, “We continue to make significant progress in our pivotal global Phase III clinical trial of Multikine (Leukocyte Interleukin, Injection). We believe that we are well positioned both financially and operationally to support ongoing clinical activities with the goal of making Multikine a very important new treatment for head and neck cancer.” About CEL-SCI Corporation CEL-SCI is dedicated to research and development directed at improving the treatment of cancer and other diseases by utilizing the immune system, the body's natural defense system. Its lead investigational therapy is Multikine (Leukocyte Interleukin, Injection), currently being studied in a pivotal global Phase III clinical trial. CEL-SCI is also developing (and investigating) an immunotherapy (LEAPS-H1N1-DC) as a possible treatment for H1N1 hospitalized patients and as a vaccine (CEL-2000) for Rheumatoid Arthritis (currently in preclinical testing) using its LEAPS technology platform. The investigational immunotherapy LEAPS-H1N1-DC treatment involves non-changing regions of H1N1 Pandemic Flu, Avian Flu (H5N1), and the Spanish Flu, as CEL-SCI scientists are very concerned about the possible emergence of a new more virulent hybrid virus through the combination of H1N1 and Avian Flu, or maybe Spanish Flu. The Company has operations in Vienna, Virginia, and in/near Baltimore, Maryland.
For more information, please visit www.cel-sci.com.Multikine is the trademark that CEL-SCI has registered for this investigational therapy, and this proprietary name is subject to FDA review in connection with our future anticipated regulatory submission for approval. Multikine has not been licensed or approved for sale, barter or exchange by the FDA or any other regulatory agency. Similarly, its safety or efficacy has not been established for any use. Moreover, no definitive conclusions can be drawn from the early-phase, clinical-trials data involving the investigational therapy Multikine (Leukocyte Interleukin, Injection). Further research is required, and early-phase clinical trial results must be confirmed in the well-controlled, Phase III clinical trial of this investigational therapy that is currently in progress. When used in this report, the words "intends," "believes," "anticipated", “plans” and "expects" and similar expressions are intended to identify forward-looking statements. Such statements are subject to risks and uncertainties which could cause actual results to differ materially from those projected. Factors that could cause or contribute to such differences include, an inability to duplicate the clinical results demonstrated in clinical studies, timely development of any potential products that can be shown to be safe and effective, receiving necessary regulatory approvals, difficulties in manufacturing any of the Company's potential products, inability to raise the necessary capital and the risk factors set forth from time to time in CEL-SCI Corporation's SEC filings, including but not limited to its report on Form 10- K for the year ended September 30, 2012. The Company undertakes no obligation to publicly release the result of any revision to these forward-looking statements which may be made to reflect the events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.
|CONSOLIDATED STATEMENTS OF OPERATIONS|
|THREE MONTHS ENDED DECEMBER 31, 2012 AND 2011|
|GRANT INCOME AND OTHER||$||15,000||$||5,024|
|Research and development (excluding R&D depreciation of $109,545 and $114,612 respectively, included below)||2,924,722||2,456,185|
|Depreciation and amortization||133,450||138,425|
|General & administrative||2,001,285||1,853,690|
|Total operating expenses||5,059,457||4,448,300|
|GAIN ON DERIVATIVE INSTRUMENTS||2,746,198||956,470|
|ISSUANCE OF ADDITIONAL SHARES DUE TO RESET PROVISIONS||-||(250,000||)|
|MODIFICATIONS OF WARRANTS||-||(325,620||)|
|NET LOSS AVAILABLE TO COMMON SHAREHOLDERS||$||(2,310,246||)||$||(4,156,833||)|
|NET LOSS PER COMMON SHARE|
|WEIGHTED AVERAGE COMMON SHARES OUTSTANDING|